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We are currently looking for a Automation Technician to join a leading pharmaceutical company based in Hertfordshire.
As the Automation Technician, you will be responsible for ensuring the smooth operation and maintenance of automation systems within a production environment.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Automation Technician will be varied; however, the key duties and responsibilities are as follows:
1.
As an Automation Technician, you will provide support for automation systems, ensuring they operate efficiently and effectively.
2.
As an Automation Technician, you will conduct routine maintenance and troubleshooting of control and instrumentation equipment.
3.
As an Automation Technician, you will collaborate with the production team to optimise automation processes.
4.
As an Automation Technician, you will assist in the implementation of new automation projects and upgrades.
ROLE REQUIREMENTS:
To be successful in your application to this exciting role as the Automation Technician, we are looking to identify the following on your profile and past history:
1.
Relevant degree in a related field such as Electrical Engineering, Automation, or similar.
2.
Proven industry experience in a pharmaceutical or similar production environment.
3.
A working knowledge and practical experience with control and instrumentation systems, such as Siemens, DeltaV or similar production-related control systems/automation.
Key Words:
Control & Instrumentation / Automation Technician / Pharmaceutical Production / Automation Support / Control Systems / Instrumentation Maintenance / Production Environment/ Automation Projects / Control & Instrumentation Technician/ Hertfordshire/ GMP/ Production
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer.
We welcome applications from anyone who meets the role requirements.
HRS exclusively supports the Life Science sectors, combining recruitment expertise with scientific knowledge to help you advance your career. ....Read more...
Type: Contract Location: Hertfordshire,England
Start: 13/11/2025
Duration: 6 months
Salary / Rate: Competitive
Posted: 2025-11-13 11:33:11
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Our client is seeking a dedicated and innovative Research Scientist to join a leading biopharmaceutical company based in the Berkshire area.
As a Research Scientist, you will be responsible for advancing small-scale antibody production and automation within the Antibody Production Sciences group.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Research Scientist will be varied however the key duties and responsibilities are as follows:
1. As a Research Scientist, you will perform small-scale transient mammalian transfections and purify monoclonal antibodies using automated techniques.
2.
As a Research Scientist, you will troubleshoot purification and quality issues, interpret data, and propose creative solutions to ensure the delivery of high-quality reagents.
3.
As a Research Scientist, you will lead and support the development, optimisation, and implementation of automated/robotic high-throughput platforms for antibody expression and purification.
4.
As a Research Scientist, you will apply data analysis and visualisation tools to improve workflows and troubleshoot bottlenecks.
ROLE REQUIREMENTS:
To be successful in your application to this exciting role as the Research Scientist we are looking to identify the following on your profile and past history:
1.
Relevant degree in Biochemistry, Biotechnology, or related fields.
2.
Proven industry experience in cell culture, antibody expression, purification, or characterisation.
3.
A working knowledge and practical experience with protein biochemistry, purification techniques, and analytical methods.
Key Words:
Research Scientist / Antibody Production / Biotechnology / Small-Scale Production / Automation / Mammalian Cell Culture / Protein Purification / Data Analysis / Machine Learning / Biochemistry
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer.
We welcome applications from anyone who meets the role requirements.
HRS exclusively supports the Life Science sectors, combining recruitment expertise with scientific knowledge to help you advance your career. ....Read more...
Type: Contract Location: Berkshire,England
Start: 06/11/2025
Duration: 12 Months
Salary / Rate: £20 - £24.50 per hour
Posted: 2025-11-06 09:52:03
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Our client, a leading Pharmaceutical Company in Cambridgeshire, is seeking a Quality Engineer to join their team on an initial 12 month contract.
As the Quality Engineer, you will be responsible for providing subject matter expertise to medical device and combination product development programmes throughout the product lifecycle.
This role offers hybrid working (50% onsite).
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Quality Engineer will be varied however the key duties and responsibilities are as follows:
1.
As the Quality Engineer, you will lead design control and risk management activities for combination product development programmes, ensuring deliverables are appropriately authored, approved, and maintained to support clinical trials and commercial licensures.
2.
As the Quality Engineer, you will support and facilitate effective risk management activities at external design companies and manufacturing facilities related to assigned projects.
3.
As the Quality Engineer, you will ensure combination product development activities are compliant with quality and regulatory standards, both internal and external.
4.
As the Quality Engineer, you will provide input and support to design validation including, but not limited to, human factors engineering assessments.
ROLE REQUIREMENTS:
To be successful in your application to this exciting role as the Quality Engineer we are looking to identify the following on your profile and past history:
1.
Relevant degree in a science or engineering discipline such as chemistry, biology, biomedical sciences, mechanical engineering, materials sciences, or chemical engineering.
2.
Proven industry experience in the pharmaceutical combination product and/or device industries.
3.
A working knowledge and practical experience with ISO 13485, ISO 14971, 21 CFR 820, 21 CFR 4, and the EU Medical Devices Regulation.
Key Words:
Design Control / Risk Management / Medical Device / Combination Product / Pharmaceutical / Cambridge / Quality Standards / Regulatory Compliance / Human Factors Engineering
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer.
We welcome applications from anyone who meets the role requirements.
HRS exclusively supports the Life Science sectors, combining recruitment expertise with scientific knowledge to help you advance your career. ....Read more...
Type: Contract Location: Cambridgeshire,England
Start: 04/11/2025
Duration: 12 months
Salary / Rate: £20 - £26 per hour
Posted: 2025-11-04 16:07:04
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ROLE OVERVIEW
We are currently looking for an Surface Modification Scientist to join a leading scientific company based in the Oxfordshire area.
As the Surface Modification Scientist, you will be responsible for driving the development and expansion of innovative coating chemistries to support various projects.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Surface Modification Scientist will be varied; however, the key duties and responsibilities are as follows:
1.
Conduct practical lab-based work focused on current and new product R&D programmes linked to customer and emerging market needs.
2.
Engage in R&D to extend the companys core platform and IP portfolio, involving testing and analytical work across various substrates and material forms.
3.
Perform technical evaluation of results for further surface treatment development and broader application of experience and knowledge for product development purposes.
4.
Conduct literature and market research to support current and future R&D programs, and prepare/review technical documents.
ROLE REQUIREMENTS:
To be successful in your application to this exciting role as the Surface Modification Scientist, we are looking to identify the following on your profile and past history:
1.
Relevant degree in chemistry (i.e.
Organic Chemistry, Synthetic Chemistry, Formulation Chemistry) with proven industry experience in polymeric membrane development and membrane separation processes.
2.
A working knowledge and practical experience with organic chemistry, organic synthesis, coating development, or formulation is expected on application.
Key Words: Surface Modification Scientist / Applications Scientist / R&D / Chemistry / Coating Chemistries / Membrane Development / Surface Treatment / Organic Synthesis / Product Development / Laboratory Work / Analytical Work
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer.
We welcome applications from anyone who meets the role requirements.
HRS exclusively supports the Life Science sectors, combining recruitment expertise with scientific knowledge to help you advance your career. ....Read more...
Type: Permanent Location: Islip,England
Start: 29/10/2025
Salary / Rate: Competitive
Posted: 2025-10-29 19:12:04
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ROLE OVERVIEW
Our client, a leading company in the scientific research industry, is currently seeking a Laboratory Technician on a temporary contact to join their team based in Cheshire.
As a Laboratory Technician, you will play a crucial role in supporting the daily operations of the laboratory, ensuring a smooth and efficient working environment for the scientists.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Laboratory Technician will be varied however the key duties and responsibilities are as follows:
1.
General laboratory housekeeping, including cleaning, freezer maintenance, and maintaining laboratory glassware.
Ensuring the working area is kept orderly and consumables are available for current and future work.
2.
Daily collection and disposal of waste from labs, ensuring proper disposal of hazardous and biological waste.
3.
Preparation of standard analytical solutions, buffers, and media used by scientists within the laboratories.
4.
Monitoring and reporting equipment issues to the Facilities Manager, arranging repair and maintenance, and documenting maintenance activities.
ROLE REQUIREMENTS:
To be successful in your application to this exciting role as the Laboratory Technician we are looking to identify the following on your profile and past history:
1.
Relevant degree in a biological science subject or equivalent qualification.
2.
Proven industry experience in a laboratory environment.
3.
A working knowledge and practical experience with laboratory housekeeping and preparation of analytical solutions.
Key Words: Laboratory Technician / Lab Support / Research Laboratory / Scientific Research / Biological Science / Lab Maintenance / Analytical Solutions / Lab Housekeeping / Laboratory Consumables / Lab Equipment Maintenance
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer.
We welcome applications from anyone who meets the role requirements.
HRS exclusively supports the Life Science sectors, combining recruitment expertise with scientific knowledge to help you advance your career. ....Read more...
Type: Contract Location: Cheshire,England
Start: 28/10/2025
Salary / Rate: Competitive
Posted: 2025-10-28 15:36:03
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ROLE OVERVIEW
An exciting opportunity for a VP, Global Regulatory Affairs to join a leading Cell and Gene Therapy CDMO.
As the VP, Global Regulatory Affairs, you will play a key role in providing global regulatory leadership, supporting clients developing advanced therapy programmes from early development through to commercialisation.
You will be responsible for defining and implementing global regulatory strategies, ensuring compliance with international standards, and building strong partnerships with regulatory authorities.
This role reports directly into the SVP, Global Quality and will lead an experienced regulatory team during a period of continued international growth.
KEY DUTIES AND RESPONSIBILITIES
Your duties as the VP, Global Regulatory Affairs will be varied however the key duties and responsibilities are as follows:
- Develop and execute global regulatory strategies that support client programmes across cell and gene therapy, ensuring alignment with regional and international agency expectations.
- Act as the senior regulatory representative with global health authorities, leading discussions, responses, and inspections while building trusted long-term relationships.
- Provide expert regulatory input across CMC, clinical, and post-approval activities, supporting high-quality submissions such as INDs, IMPDs, and variations.
- Partner with commercial, quality, and technical operations teams to provide regulatory insight during client engagements, business development activities, and due diligence reviews.
- Lead, coach, and mentor a high-performing global regulatory team, fostering collaboration, accountability, and professional development across regions.
ROLE REQUIREMENTS
To be successful in your application to this exciting role as the VP, Global Regulatory Affairs we are looking to identify the following on your profile and past history:
- A Degree or higher level in a relevant Life Science discipline (e.g., Pharmaceutical Chemistry / Biochemistry / Regulatory Science).
- Extensive experience in global regulatory affairs within biologics, advanced therapy, or gene therapy environments.
- Proven leadership experience within a CDMO or partnering organisation, managing regulatory teams and engaging with global health authorities.
- Demonstrated ability to lead strategic regulatory initiatives, ensuring compliance and supporting clients through the product lifecycle.
WHATS IN IT FOR YOU?
You will join a business recognised for its expertise in advanced therapies and biologics manufacturing, with the opportunity to shape global regulatory strategy across a growing international network. This position offers visibility at executive level, direct involvement in client partnerships, and the chance to influence regulatory direction in one of the most innovative areas of life sciences.
You will be part of the senior leadership team driving excellence in Cell and Gene Therapy development.
KEY WORDS: VP Global Regulatory Affairs / Regulatory Affairs / Advanced Therapy / Gene Therapy / Biologics / ATMP / CGT / CDMO / CMC / FDA / EMA / MHRA / Leadership / Compliance / Regulatory Strategy / Quality Systems / Biotechnology
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer.
We welcome applications from anyone who meets the role requirements.
HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career. ....Read more...
Type: Permanent Location: Oxfordshire,England
Start: 06/10/2025
Salary / Rate: Experience Dependent
Posted: 2025-10-06 11:39:11
